MicroRNA-221 and -222 pathway controls melanoma progression

被引:61
作者
Felicetti, Federica [1 ]
Errico, M. Cristina [1 ]
Segnalini, Patrizia [1 ]
Mattia, Gianfranco [1 ]
Care, Alessandra [1 ]
机构
[1] Ist Super Sanita, Dept Hematol Oncol & Mol Med, I-00161 Rome, Italy
关键词
antagomir; c-KIT; melanoma; microRNA; p27Kip; tumor progression;
D O I
10.1586/14737140.8.11.1759
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) represent a new family of small noncoding RNAs that negatively regulate gene expression. Recent studies demonstrated miRNA involvement in all the main biological processes, including tumor development as a consequence of an aberrant deregulated expression. Growing evidence is showing the capability of miRNA expression profiles to unequivocally distinguish between normal and neoplastic tissues, leading to the identification of new diagnostic and/or prognostic molecular markers. In addition, miRNAs might eventually represent new targets to aim at as innovative therapeutic approaches, particularly relevant in those types of cancer, such as melanoma, which are still lacking effective traditional therapies. In particular, the inhibition of miRNA-221 and -222, which are abnormally expressed in melanoma and favor the induction of the malignant phenotype by downregulating c-KIT receptor and p27Kip, might in the future represent an efficient treatment for translation into the clinical setting.
引用
收藏
页码:1759 / 1765
页数:7
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